# Promethean Surgical Devices, Inc.

- Location (FDA's records): East Harford, CT
- FDA decisions: 1 (2010–2010): 1 510(k) clearance
- Product codes: FTL (1)
- Predicates its devices cite: 4 (0 its own); citations of its devices by later devices: 1 (0 its own)
- Recalls linked to its devices: 0 (0 Class I)
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Firms whose devices it cites most
- Artimplant AB: 2 (https://510kreport.com/company/artimplant)
- Mentor Corp.: 1 (https://510kreport.com/company/mentor)
- Mpathy Medical Devices, Ltd.: 1 (https://510kreport.com/company/mpathy-medical-devices)

## Firms that cite its devices most
- Tyrx, Inc.: 1 (https://510kreport.com/company/tyrx)

## Its most-cited devices
- K090271: Hydrocoat Mesh (2010), cited by 1

## Recent decisions
- K090271: Hydrocoat Mesh (Jan 14, 2010)

Source page: https://510kreport.com/company/promethean-surgical-devices